FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LKB 2189 ULTROPROCESSOR

K Number: K843506 · Decision Nov 30, 1984
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
11
Applicant Total
52
Review Days
85

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Basic Information

Device Name
LKB 2189 ULTROPROCESSOR
K Number
K843506
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3875
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Lkb Instruments, Inc.
Date Received
September 6, 1984
Decision Date
November 30, 1984
Product Code
IEO
Advisory Committee
Pathology
Review Advisory Committee
PA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IEO Processor, Tissue, Automated

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K Number Device Name
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K871599 DELFIA(TM) HIGE KIT
K871644 DELFIA (TM) HTSH KIT
K864452 DELFIA(TM) TRIIODOTHYRONINE (T3) KIT
K864733 LKB 2260 MACROTOME
K862848 LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110
K863422 DELFIA(TM) CORTISOL KIT
K861195 DELFIA DIGOXIN
Search all 52 clearances from Lkb Instruments, Inc. →